Canonical Allele Identifier: PA2826425338
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1753679
ClinVar RCV Id: RCV002361922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val28983Ile
CA349496316
NM_001256850.1:c.86947G>A